/tool-data/bfast_indexes.loc.sample
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- #This is a sample file distributed with Galaxy that enables tools
- #to use a directory of BFAST indexed sequences data files. You will need
- #to create these data files and then create a bfast_indices.loc file
- #similar to this one (store it in this directory) that points to
- #the directories in which those files are stored. The bfast_indexes.loc
- #file has this format (white space characters are TAB characters):
- #
- #<unique_id> <build> <galaxy format extensions valid1,valid2> <description> <bfast_index_directory>
- #
- #
- #So, for example, if you had hg18 indexed for 40+ bp NT reads stored in
- #/galaxy/data/hg18/bfast_index/nt/40+,
- #then the bfast_indices.loc entry could look like this:
- #
- #hg18_nt_40+ hg18 fastqsanger hg18: 40+ bp NT Space reads /galaxy/data/hg18/bfast_index/nt/40+/hg18.fa
- #
- #and your /depot/data2/galaxy/hg18/bfast/nt/40+ directory
- #would contain hg18.fa.*.brg and hg18.fa.*.bif files:
- #hg18.fa.nt.brg
- #hg18.fa.nt.1.1.bif
- #hg18.fa.nt.2.1.bif
- #...etc...
- #or similarly for color space indexes:
- #hg18.fa.nt.brg #NB: the localalign process requires the nucleotide brg file
- #hg18.fa.cs.brg
- #hg18.fa.cs.1.1.bif
- #hg18.fa.cs.2.1.bif
- #...etc...
- #
- #a 'generic' directory can be used to hold intermixed NT and CS indexes, when differentiating is not needed, the bfast_indices.loc entry could look like this:
- #hg18_standard hg18 fastqsanger,fastqcssanger hg18 standard indexes /galaxy/data/hg18/bfast_index/hg18.fa
- #
- #The use of symlinks to prevent copying of e.g. .fa and .brg files is recommended
- #
- #hg18_nt_40+ hg18 fastqsanger hg18: 40+ bp NT Space reads /galaxy/data/hg18/bfast_index/nt/40+/hg18.fa
- #hg18_cs_50+ hg18 fastqcssanger hg18: 50+ bp Color space reads /galaxy/data/hg18/bfast_index/cs/50+/hg18.fa
- #hg18_nt_40- hg18 fastqsanger hg18: 40- bp NT Space reads /galaxy/data/hg18/bfast_index/nt/40-/hg18.fa
- #phiX_nt_50 phiX fastqsanger phiX: 50 bp NT Space reads /galaxy/data/phiX/bfast_index/nt/50/phiX.fa